Pharbetol
- Product NDC
- 16103-353
- 11-digit product format
- 161030353
- Labeler code
- 16103
- Product ID
- 16103-353_c23d82e7-ab4d-4bda-b63d-cc7f96bb79f6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Pharbest Pharmaceuticals, Inc.
- Application
- M013
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2007-01-09
- Substance
- ACETAMINOPHEN
- Active strength
- 325 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Observed NDC auxiliary status history#
This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
| Captured / source date | Dataset | Scope | Package NDC | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|
| 2020-12-18 03:04 UTC · source 2020-12-17 | excluded product | product | e2bbac7714bc… | 27bdfed8d636… | |
| 2020-12-18 03:04 UTC · source 2020-12-17 | excluded package | package | 16103-353-07 | e2bbac7714bc… | 27bdfed8d636… |
| 2020-12-18 03:04 UTC · source 2020-12-17 | excluded package | package | 16103-353-08 | e2bbac7714bc… | 27bdfed8d636… |
| 2020-12-18 03:04 UTC · source 2020-12-17 | excluded package | package | 16103-353-11 | e2bbac7714bc… | 27bdfed8d636… |
| 2020-06-10 20:45 UTC · source 2020-06-10 | excluded product | product | 9bebd1f3094a… | 5416666fcb17… | |
| 2020-06-10 20:45 UTC · source 2020-06-10 | excluded package | package | 16103-353-07 | 9bebd1f3094a… | 5416666fcb17… |
| 2020-06-10 20:45 UTC · source 2020-06-10 | excluded package | package | 16103-353-08 | 9bebd1f3094a… | 5416666fcb17… |
| 2020-06-10 20:45 UTC · source 2020-06-10 | excluded package | package | 16103-353-11 | 9bebd1f3094a… | 5416666fcb17… |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Pharbetol
- Brand name suffix
- Regular strength
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| ACETAMINOPHEN | 325 mg/1 |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 362O9ITL9D | Internal UNII lookup |
Harmonized RxCUI identifiers#
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| e0a39957-d918-4125-88f9-0e550b976fa1 | Available on FDA.report |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Related label |
|---|---|---|
| 16103-353-07 | 2026-01-29 | Drug Facts |
| 16103-353-08 | 2026-01-29 | Drug Facts |
| 16103-353-11 | 2026-01-29 | Drug Facts |
| 16103-353-07 | 2023-06-13 | Drug Facts |
| 16103-353-08 | 2023-06-13 | Drug Facts |
| 16103-353-11 | 2023-06-13 | Drug Facts |
| 16103-353-07 | 2023-01-30 | Drug Facts |
| 16103-353-08 | 2023-01-30 | Drug Facts |
| 16103-353-11 | 2023-01-30 | Drug Facts |
| 16103-353-07 | 2021-01-08 | Drug Facts |
| 16103-353-08 | 2021-01-08 | Drug Facts |
| 16103-353-11 | 2021-01-08 | Drug Facts |
| 16103-353-07 | 2020-01-31 | Drug Facts |
| 16103-353-08 | 2020-01-31 | Drug Facts |
| 16103-353-11 | 2020-01-31 | Drug Facts |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 16103-353-07 | PharbetolRegular strength | 60 in 1 BOTTLE, PLASTIC | TABLET | 60 | 5 | |
| 16103-353-07 | PharbetolRegular strength | 1 in 1 CARTON | TABLET | 1 | 5 | |
| 16103-353-08 | PharbetolRegular strength | 100 in 1 BOTTLE, PLASTIC | TABLET | 100 | 5 | |
| 16103-353-08 | PharbetolRegular strength | 1 in 1 CARTON | TABLET | 1 | 5 | |
| 16103-353-11 | PharbetolRegular strength | 1000 in 1 BOTTLE | TABLET | 1000 | 5 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 16103-353-07 | EA - Each | 16103-353 | be19f1cb-5a83-4ab8-a81c-dbc7b6c366b3 | 1 | 2013-05-02 |
| 16103-353-08 | EA - Each | 16103-353 | d0efd342-8f78-4b8b-b2ab-963c13f461bf | 1 | 2013-05-02 |
| 16103-353-11 | EA - Each | 16103-353 | 239e09b4-a5bc-4312-a3cc-d82250536ba3 | 1 | 2013-05-02 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| MAXIMUM STRENGTH NON-ASPIRIN 100 | ACETAMINOPHEN | JHK Inc dba American Safety & First Aid | 1d3e9948-883e-4668-9bb8-d699a283b51a | 2025-12-16 | Warnings | M013 |
| TYLENOL EXTRA STRENGTH, TRAVEL BASIX | ACETAMINOPHEN | Lil' Drug Store Products, Inc. | fa951d50-b79c-4161-8c81-fcf386b0964e | 2025-12-15 | Warnings | M013 |
| Vanquish Extra Strength | ACETAMINOPHEN, ASPIRIN, AND CAFFEINE | DSE Healthcare Solutions, LLC | cbf12223-ef44-494b-9d3c-971dce3c5ade | 2025-12-15 | Warnings | M013 |
| Low Dose Aspirin | ASPIRIN | CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED | 8bc75bcf-01c9-41d0-a96f-77a24e3edf01 | 2025-12-15 | Warnings | M013 |
| Pain Reliever | ACETAMINOPHEN | WALGREENS | 40a1b354-9b2e-1cf3-e063-6394a90af113 | 2025-12-13 | Warnings | M013 |
| topcare childrens pain and fever | ACETAMINOPHEN | Topco Associates LLC | 911492d5-e065-4b8f-b2dc-cb6a6678d0ae | 2025-12-13 | Warnings | M013 |
| Pain Reliever, Extra Strength, 24-7 Life by 7-Eleven | ACETAMINOPHEN TABLET | Lil' Drug Store Products, Inc. | 45c397bd-a1ff-1246-e063-6394a90ac54a | 2025-12-12 | Warnings | M013 |
| Pain Reliever PM, Extra Strength, 24-7 Life by 7-Eleven | ACETAMINOPHEN, DIPHENHYDRAMINE HCL TABLET, FILM COATED | Lil' Drug Store Products, Inc. | 45c7c11b-d627-aee8-e063-6294a90a401d | 2025-12-12 | Warnings | M013 |
| Aspirin | ASPIRIN | TOP CARE (Topco Associates LLC) | d3df90be-9037-44b2-bf48-540d68a033b2 | 2025-12-12 | Warnings | M013 |
| Low Dose Aspirin | ASPIRIN | Hy-Vee | 98ab6fb7-c7e5-45ab-97c3-81d422f8a843 | 2025-12-11 | Warnings | M013 |
| Acetaminophen | ACETAMINOPHEN | PAI Holdings, LLC dba PAI Pharma | 33599f18-5f49-4f22-8a77-a072115763ef | 2025-12-11 | Warnings | M013 |
| Low Dose Aspirin | ASPIRIN | VALU MERCHANDISERS COMPANY | 746059b3-ed18-4a81-a70e-4d758e048d8e | 2025-12-11 | Warnings | M013 |
| Extra Strength Pain Relief PM | ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE | VALU MERCHANDISERS COMPANY | f8820150-feec-4062-85bb-14525ddf691f | 2025-12-11 | Warnings | M013 |
| Extra Strength Pain Relief | ACETAMINOPHEN | VALU MERCHANDISERS COMPANY | 005e299e-aa84-49d9-bbca-12236f865a27 | 2025-12-11 | Warnings | M013 |
| Low Dose Chewable Aspirin | ASPIRIN | VALU MERCHANDISERS COMPANY | 7d88f156-d361-4249-b70d-4bbcd5ba30b7 | 2025-12-11 | Warnings | M013 |
| Enteric Coated Aspirin | ASPIRIN | VALU MERCHANDISERS COMPANY | cc18e8e1-652e-44da-a9d7-e56cebda55a1 | 2025-12-11 | Warnings | M013 |
| Extra Strength Pain Relief | ACETAMINOPHEN | VALU MERCHANDISERS COMPANY | d4c32e70-778a-4d66-b9d0-03944a528421 | 2025-12-11 | Warnings | M013 |
| adult low dose aspirin | ASPIRIN | VALU MERCHANDISERS COMPANY | 6fa1c707-bd42-455b-90a3-2c2a11acc683 | 2025-12-11 | Warnings | M013 |
| Extra Strength Pain Relief | ACETAMINOPHEN | VALU MERCHANDISERS COMPANY | 5a80cb17-7731-4457-acd3-64cf4accf862 | 2025-12-11 | Warnings | M013 |
| Acetaminophen | ACETAMINOPHEN | VALU MERCHANDISERS COMPANY | 02e3798f-86d9-64b4-e063-6294a90a29de | 2025-12-11 | Warnings | M013 |
DailyMed RxNorm Mappings#
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 16103-353-07 | 16103035307 | 1 BOTTLE, PLASTIC in 1 CARTON (16103-353-07) / 60 TABLET in 1 BOTTLE, PLASTIC | 2007-01-09 | 0000-00-00 | No | No | Current | |
| 16103-353-08 | 16103035308 | 1 BOTTLE, PLASTIC in 1 CARTON (16103-353-08) / 100 TABLET in 1 BOTTLE, PLASTIC | 2007-01-09 | 0000-00-00 | No | No | Current | |
| 16103-353-11 | 16103035311 | 1000 TABLET in 1 BOTTLE (16103-353-11) | 1000 tablet | 2007-01-09 | 0000-00-00 | No | No | Current |